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  1. 1
    Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia

    Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalass... von Hantaweepant, Chattree, Suktitipat, Bhoom, Pithukpakorn, Manop, Chinthammitr, Yingyong, Limwongse, Chanin, Tansiri, Nawaporn, Sawatnatee, Surasak, Takpradit, Chayamon, Rotchanapanya, Wannaphorn, Pongudom, Saranya, Charoenprasert, Kanyaporn, Paiboonsukwong, Kittiphong, Thamprasert, Wichuda, Nolwachai, Narumol, Rattanasawat, Wanlapa, Sae-Aeng, Busakorn, Khorwanichakij, Nisachon, Saetow, Putchong, Saengboon, Supawee, Kamjornpreecha, Krittichat, Pholmoo, Wikanda, Dujjawan, Boonyanuch, Siritanaratkul, Noppadol

    Veröffentlicht in Hematology (Luxembourg)

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  2. 2
    Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia

    Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalass... von Hantaweepant, Chattree, Suktitipat, Bhoom, Pithukpakorn, Manop, Chinthammitr, Yingyong, Limwongse, Chanin, Tansiri, Nawaporn, Sawatnatee, Surasak, Takpradit, Chayamon, Rotchanapanya, Wannaphorn, Pongudom, Saranya, Charoenprasert, Kanyaporn, Paiboonsukwong, Kittiphong, Thamprasert, Wichuda, Nolwachai, Narumol, Rattanasawat, Wanlapa, Sae-Aeng, Busakorn, Khorwanichakij, Nisachon, Saetow, Putchong, Saengboon, Supawee, Kamjornpreecha, Krittichat, Pholmoo, Wikanda, Dujjawan, Boonyanuch, Siritanaratkul, Noppadol

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